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WO2004029175A1 - Produit de traitement de trous de forage contenant une phase huileuse a faible toxicite - Google Patents

Produit de traitement de trous de forage contenant une phase huileuse a faible toxicite Download PDF

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Publication number
WO2004029175A1
WO2004029175A1 PCT/EP2003/009981 EP0309981W WO2004029175A1 WO 2004029175 A1 WO2004029175 A1 WO 2004029175A1 EP 0309981 W EP0309981 W EP 0309981W WO 2004029175 A1 WO2004029175 A1 WO 2004029175A1
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WO
WIPO (PCT)
Prior art keywords
treatment agent
oil phase
linear
atoms
saturated
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2003/009981
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German (de)
English (en)
Inventor
Heinz Müller
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF Personal Care and Nutrition GmbH
Original Assignee
Cognis Deutschland GmbH and Co KG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Cognis Deutschland GmbH and Co KG filed Critical Cognis Deutschland GmbH and Co KG
Priority to US10/527,212 priority Critical patent/US7666820B2/en
Priority to MXPA05002670A priority patent/MXPA05002670A/es
Priority to EP03769267A priority patent/EP1546282B1/fr
Priority to DE50304776T priority patent/DE50304776D1/de
Priority to CA002499667A priority patent/CA2499667A1/fr
Priority to BRPI0314586-7A priority patent/BR0314586B1/pt
Priority to AU2003277848A priority patent/AU2003277848B2/en
Publication of WO2004029175A1 publication Critical patent/WO2004029175A1/fr
Anticipated expiration legal-status Critical
Priority to NO20051862A priority patent/NO339445B1/no
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/02—Well-drilling compositions
    • C09K8/32—Non-aqueous well-drilling compositions, e.g. oil-based
    • C09K8/34—Organic liquids
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/02—Well-drilling compositions
    • C09K8/32—Non-aqueous well-drilling compositions, e.g. oil-based
    • C09K8/36—Water-in-oil emulsions
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S507/00—Earth boring, well treating, and oil field chemistry
    • Y10S507/905—Nontoxic composition

Definitions

  • the invention describes borehole treatment compositions which contain an aqueous phase and an oil phase, this oil phase having particularly low toxicity values in relation to marine microorganisms.
  • Well treatment products are all types of auxiliary fluids that can be used in the drilling of oil or gas deposits. As a characteristic example of such
  • the invention describes treatment agents in the following on the basis of drilling fluids and drilling muds based thereon, which can be used in both land-based and sea-based drilling.
  • auxiliary fluids of the type concerned here
  • the numerous other auxiliary fluids in the subject area mentioned here come into consideration. Examples include spotting fluids, spacers, packer fluids,
  • the invention includes both auxiliary liquids of the type mentioned, which are oil-based, i.e. work with a closed oil phase, as well as aids in which the oil phase is emulsified in a particularly aqueous closed phase. Drilling fluids or based on them
  • Drilling muds are characteristic examples of the different possibilities.
  • water-based drilling fluids containing approximately 1 to 50% emulsified oil phase are known - in addition to the other conventional auxiliaries of such a drilling fluid - which are also referred to as O / W emulsion fluids.
  • oil-based flushing systems are widely used, in which the oil forms the flowable phase or at least a substantial proportion of the flowable phase as a closed oil phase.
  • the so-called invert drilling muds which contain a disperse aqueous phase in the closed oil phase based on W / O emulsions, are of particular importance here.
  • the content of the disperse aqueous phase is usually in the range from at least about 5 to 10% by weight to about 50 to 60% by weight.
  • the so-called true oil muds are also known, the liquid phase of which is formed almost exclusively from a closed oil phase, which at most only small amounts - usually not more than about 5 to 10 wt .-% - contain dispersed in aqueous phase.
  • the non-aqueous phase of such flushing systems is formed by the so-called carrier fluid. It is usually diesel oil which, when mixed with certain additives, forms the actual drilling fluid.
  • carrier fluids At the end of the eighties, however, there was a need for environmentally friendly flushing systems and therefore carrier fluids. In particular, these should be more biodegradable than the diesel oil used to date.
  • the toxicity of a rinse is usually determined using biological tests in which marine microorganisms are exposed to the components of the rinse in different concentrations. The aim is to find flushing systems that both meet the physical and technical requirements and have the lowest possible toxicity to the environment. At this point it should also be noted the physical loads on the drilling fluids.
  • the rinses are heated in large baptisms to high temperatures, up to 250 C C and more, there are high pressures and the compounds of the rinse must both remain chemically stable and have no significant change in their viscosity behavior, and furthermore also under the form a stable emulsion.
  • the object of the present invention was to provide borehole treatment agents, in particular drilling fluids, which are improved both in terms of their application properties and in terms of their ecological compatibility.
  • the present application therefore relates to borehole treatment compositions containing an aqueous phase and a non-aqueous oil phase, emulsifiers and, if appropriate, other customary additives, such as, for example, weighting agents, fluid-loss additives, viscosity-regulating additives, wetting agents, salts, biocides, corrosion inhibitors, and / or an alkali reserve, the non-aqueous phase being selected in whole or in part from the group of a) paraffins with 5 to 22 carbon atoms and / or, b) internal olefins with 12 to 30 carbon atoms in the molecule, each in admixture with c) carboxylic acid esters of the general formula R-COO-R ', in which R is a linear or branched, saturated or unsaturated alkyl radical having 15 to 25 C atoms and R 'is a saturated, linear or branched alkyl radical having 3 to 22 C atoms, or from mixtures of components a)
  • the Environmental Protection Agency prescribes the toxicity test using the above-mentioned leptocheirus test according to ASTM E 1367 for such drilling fluid systems that are to be used for drilling in the Gulf of Mexico.
  • the toxicity for a standard compound namely a mixture of internal olefins of the chain lengths C16 / C18, is compared with the results of the carrier fluids to be tested.
  • the rinses according to the invention contain oil phases whose value for F is less than 1, preferably less than 0.5, and in special cases less than 0.4.
  • esters - based on total C chain C16 - C26 are able to adjust the overall toxicity for mixtures of hydrocarbons with esters to the criteria required by the EPA.
  • Exemplary mashes with their F values are listed below:
  • OMC586 means a 2-ethylhexanol ester based on saturated fatty acids C8-C14.
  • OMC233 corresponds to an isobutanol ester based on the C14-18 + C16-18 unsaturated fatty acids.
  • OMC1049 means a 2-ethylhexyl octanoate. All products from Cognis.
  • the oil phases of the systems according to the invention contain components a) and / or b) alone or together in a mixture with esters c) and, if appropriate, in a mixture with other suitable oil phases.
  • linear or branched paraffins having 5 to 22 carbon atoms are used as component a).
  • Paraffins - more correctly referred to as alkanes - are known to be saturated hydrocarbons, which for the linear or branched representatives follow the general empirical formula C n H2n + ⁇ .
  • the cyclic alkanes follow the general empirical formula C n H2n.
  • the linear and branched paraffins are particularly preferred, whereas cyclic paraffins are less preferred.
  • the use of branched paraffins is particularly preferred.
  • paraffins that are liquid at room temperature ie those with 5 to 16 carbon atoms per molecule.
  • paraffins with 17 to 22 carbon atoms which have a waxy consistency.
  • mixtures of the different paraffins it being particularly preferred if these mixtures are still liquid at 21.degree.
  • Such mixtures can be formed, for example, from paraffins with 10 to 21 carbon atoms.
  • toxicity especially in the Leptocheirus plumulosus test, paraffins alone usually do not score sufficiently.
  • Typical F values for paraffins are between 2.7 and 4.53.
  • IO Internal olefins
  • 10's are also compounds which are known per se and can be prepared by all the processes known to those skilled in the art.
  • EP 0 787 706 A1 describes, for example, a process for the synthesis of 10s by isomerization of alpha-olefins to sulfonic or persulfonic acids. It is characteristic that the IO thus obtained are linear and contain at least one olefinic double bond which is not in the alpha Position of the alkyl chain is.
  • IO or IO mixtures are used according to the invention which contain IO with 12 to 30 C atoms in the molecule, preferably with 14 to 24 C atoms and in particular with up to 20 C atoms in the molecule.
  • the Olefins used according to the invention have only one olefinic double bond.
  • the Leptocheirus test typically achieves F values between 1, 1 and 2.0.
  • esters of the general formula R-COO-R ' in which R represents a linear or branched, saturated or unsaturated alkyl radical having 15 to 25 carbon atoms and R' is a saturated, linear or branched alkyl radical having 6 to 22 carbon atoms means part of the oil phases according to the invention.
  • esters are also known chemical compounds. Their basic use in drilling fluids is e.g. Subject of EP 0 374 672 A1 or EP 0 374 671 A1.
  • the leptocheirus values for esters are typically in the range from 1.5 to 0.2, so that such compounds alone can be suitable for the formation of low-toxicity oil phases. However, certain chain lengths must be selected for this.
  • esters of which the radical R is a saturated or unsaturated alkyl radical having 15 to 25 and R 'is a saturated alkyl radical having 3 to 10 C atoms.
  • the saturated compounds are particularly preferred. It is preferred within the scope of the inventive teaching that in addition to the esters as described above, the oil phase contains a maximum of 15% by weight (based on the oil phase) of other esters with radicals R which represent alkyl radicals with more than 23 carbon atoms ,
  • Another object of the present invention therefore relates to drilling fluids which, in addition to the aqueous phase as oil phase, contain only those esters of the above general formula whose toxicity, measured according to the leptocheirus test, is less than 1 in comparison to the standard IO.
  • the present application therefore also claims drilling fluids containing an aqueous phase and a non-aqueous oil phase, emulsifiers and, if appropriate, other customary additives, such as, for example, weighting agents, fluid-loss additives, viscosity-regulating additives, wetting agents, salts, biocides, corrosion inhibitors, and / or an alkali reserve, the non-aqueous phase being selected to more than 50% by weight from the group of esters of the general formula R-COO-R 'in which R is a linear or branched, saturated or unsaturated alkyl radical having 15 to 25 C- Atoms is and R 'is a saturated, linear or branched alkyl radical with 3 to 10 carbon atoms, the non-aqueous phase having a relative toxicity, i.e.
  • esters of C1-5 monocarboxylic acids and 1- and / or polyfunctional alcohols residues of 1 -valent alcohols at least 6, preferably at least 8 C-
  • atoms and the polyhydric alcohols preferably have 2 to 6 carbon atoms in the molecule, (ii) mixtures of secondary esters selected from the group of propyl carboxylate, butyl carboxylate, pentyl carboxylate, hexyl carboxylate, heptyl carboxylate, octyl carboxylate, nonyl carboxylates, decyl carboxylate, undecyl carboxylate, dodecyl carboxylate, dodecyl carboxylate, dodecyl carboxylate
  • linear alpha-olefins of chain lengths C14 / C16 and so-called low toxicity mineral oils are excluded from the use since they do not achieve the desired toxicity values even when mixed according to the invention with esters from group c).
  • the use of diesel oil is also excluded.
  • the use of methyl esters is ruled out because, owing to their high toxicity, they are not suitable for forming low-toxic oil phases in the sense of the invention. Under certain conditions, however, it may be necessary to use such constituents, but the amounts then used are not more than 5% by weight, preferably a maximum of 2% by weight, based on the oil phase.
  • the agents according to the invention contain emulsifiers as a further mandatory component. When choosing them, it depends on the type of flushing.
  • Emulsifiers which can be used in practice to form W / O emulsions are, in particular, selected oleophilic fatty acid salts, for example those based on amidoamine compounds. Examples of this are described in the already cited US Pat. No. 4,374,737 and the literature cited therein. However, other, preferably non-ionic, emulsifiers are used to prepare W / O emulsions.
  • particularly suitable emulsifiers can be assigned to at least one of the following classes of substances: (oligo) alkoxylates - in particular low alkoxylates, in which case corresponding ethoxylates and / or propoxylates are particularly important - of lipophilic residues and for alkoxylation qualified basic molecules of natural and / or synthetic origin.
  • low means values of 2 to 15 and in particular 2 to 10 parts of alkoxide per molecule of emulsifier.
  • Another important class of nonionic emulsifiers for the purposes of the invention are partial esters and / or partial ethers of polyfunctional alcohols. in particular 2 to 6 C atoms and.2.
  • corresponding emulsifier components are alkyl (poly) glycosides of long-chain alcohols and the already mentioned fatty alcohols of natural and / or synthetic origin or alkylolamides, amine oxides and lecithins.
  • the (oligo) alkoxylates of basic molecules containing lipophilic residues can be derived in particular from selected representatives from the following classes of basic molecules containing lipophilic residues: fatty alcohols L fatty acids, Fatty amines, fatty amides, fatty acid and / or fatty alcohol esters and / or ethers, alkanolamides, alkylphenols and / or their reaction products with formaldehyde and further reaction products of carrier molecules containing lipophilic residues with lower alkoxides.
  • partial esters and / or partial ethers of polyfunctional alcohols are, in particular, the corresponding partial esters with fatty acids, for example of the type of glycerol mono- and / or diesters, glycol monoesters, corresponding partial esters of oligomerized polyfunctional alcohols, sorbitan partial esters and the like, and corresponding compounds with ether groups.
  • the oil phases are preferably formed by mixtures of components a) and / or b) with the ester oils c) in a weight ratio of 10: 1 to 1: 1, preferably 5: 1 to 1: 1 and in particular 3: 1 to 1: 1 to achieve the desired relative toxicity.
  • the downhole treatment agents of the present invention are preferably in the form of water-in-oil
  • the execution of the present agents according to the invention is particularly preferred as Drilling fluid.
  • the agents according to the invention preferably have a weight ratio between the aqueous and the oil phase of 50:50 to 1:99, preferably 30:70 to 20:80 and in particular 10:90. It is preferred that the oil phase consists of at least 50% by weight, preferably at least 80% by weight and in particular at least 90% by weight of compounds a) and / or b) and c).
  • those borehole treatment agents whose oil phase is formed at least 50% by weight, preferably at least 80% by weight and in particular 100% by weight from components a) to c).
  • the percentages by weight refer to the weight of the oil phase.
  • the non-aqueous oil phase of the agents according to the invention can be 100% by weight of mixtures of component a) and / or. b). and .c). consists.
  • the oil phases of the agents according to the invention preferably have pour points below 0 ° C., preferably below -5 ° C. (measured according to DIN ISO 3016: 1982-10).
  • the Brookfield viscosity of the oil phases is at most 50 mPas at 0 ° C.
  • the borehole treatment agents according to the invention provided they are designed as an oil-based drilling fluid of the W / O type, have a plastic viscosity (PV) in the range from 10 to 70 mPas and a yield point (YP) from 5 to 60 lb / 100 ft 2 ' determined at 50 ° C.
  • the kinematic viscosity of the oil phase measured according to Ubbelohde at 20 ° C should preferably be at most 12 mm 2 / sec.
  • the aqueous phase of the agents according to the invention preferably has a pH in the range from 7.5 to 12, preferably from 7.5 to 11 and in particular from 8 to 10.
  • the agents according to the invention also contain additives, for example weighting agents, fluid-loss additives, viscosity-regulating additives, wetting agents,
  • the additives can be water-soluble, oil-soluble and / or water- or oil-dispersible.
  • Classic additives can be: fluid loss additives, structural viscosity-building soluble and / or insoluble substances, alkali reserves, means for inhibiting the undesired water exchange between drilled formations - e.g. B water-swellable clays and / or salt layers - and the z.
  • Solid surfaces e.g. B. to improve the lubricating effect, but also to improve the oleophilic closure of exposed rock formations, or, rock surfaces, bioeides, for example to inhibit bacterial attack by O / W emulsions and the like. Accordingly, only excerpts are cited: Finely dispersed additives to increase the flushing density: Barium sulfate (barite) is widespread, but calcium carbonate (calcite) or the mixed carbonate of calcium and magnesium (dolomite) are also used.
  • lignite and lignite derivatives in particular lignosulfonates.
  • the use of toxic components is dispensed with here, the corresponding salts with toxic heavy metals such as chromium and / or copper being primarily mentioned here.
  • An example of inorganic thinners are polyphosphate compounds.
  • the additives known from the prior art for oil- and water-based drilling fluids come into consideration.
  • these are halides and / or carbonates of the alkali and / or alkaline earth metals, the corresponding potassium salts, if appropriate in combination with lime, being particularly important.
  • Alkali reserves Considering come here on the overall behavior of the mud tuned ⁇ inorganic and / or organic bases, in particular corresponding basic salts or hydroxides of alkali and / or alkaline earth metals and organic bases.
  • the use of lime (Ca (OH) 2) as an alkali reserve is particularly preferred here.
  • Typical contents of lime in the drilling fluid are between 1 and 6 Ib / bbl, whereby it depends on the type and composition of the oil phase, which quantities can be used.
  • the type and amount of these basic components are preferably selected and matched to one another such that, in the case of esters susceptible to hydrolysis, in particular unsaturated esters, the carbon number C16 to C24 no excessive hydrolysis occurs since the resulting reaction products, especially the fatty acids, can impair the stability of the emulsion drilling fluid.
  • esters susceptible to hydrolysis in particular unsaturated esters
  • the carbon number C16 to C24 no excessive hydrolysis occurs since the resulting reaction products, especially the fatty acids, can impair the stability of the emulsion drilling fluid.
  • an alkali reserve in the rinse which corresponds at most to a concentration of 2 lb / bbl of the basic component, preferably lime in the rinse under working conditions.
  • esters of group c) in admixture with components a) and / or b) leads to the fact that oil phases with low relative toxicity compared to the marine microorganism Leptocheirus plumolosus can be obtained.
  • esters of the general formula R-COO-R 'in which R represents a linear or branched, saturated or unsaturated alkyl radical having 15 to 25 carbon atoms and R' represents a saturated, linear or branched alkyl radical having 3 up to 10 carbon atoms means the lubricating properties of drilling fluids containing an aqueous phase and a non-aqueous oil phase, emulsifiers and possibly other conventional additives such as weighting agents, fluid-loss additives, viscosity regulating additives, wetting agents, salts, biocides, corrosion inhibitors, and / or an alkali reserve, significantly improved. Between 5 and 15% by weight, in particular from 8 to 12% by weight, of these esters are preferably used in the oil phase in order to achieve the desired lubrication effect.
  • esters of the general formula R-COO-R 'in which R represents a linear or branched, saturated or unsaturated alkyl radical having 15 to 25 C atoms and R' means a saturated, linear or branched alkyl radical having 3 to 10 carbon atoms the use of structuring agents, preferably products based on optionally chemically or physically modified clays, for example bentonites, for oil phases of conventional drilling fluids.
  • structuring agents preferably products based on optionally chemically or physically modified clays, for example bentonites
  • the amounts of the esters used according to the invention are between 15 and 100% by weight, preferably 25 to 100% by weight and in particular 50 to 100% by weight, based on the amount of the oil phase.
  • the proportion of structuring agents based on clay can be significantly reduced by the oil phases according to the invention. It is even possible to formulate tone-free rinses.
  • the esters are preferably used in emulsion drilling fluids of the invert type, that is to say W / O.
  • Emulsifier 8.0 bbl (EZ-Mul NTE, Baroid) fluid loss additive 8.0 bbl (Duratone HT, Baroid)
  • Oil / water ratio 80/20
  • the F value was 0.87.
  • API builetin RP 13 B-2 API builetin RP 13 B-2.
  • the rinsing of the comparative example contained only an IO mixture based on IO with C16 / C18 in the oil phase.
  • the F-value was 2.7.
  • a rinse analogous to example 1 was used for example 2, but the content of the fluid loss additive was reduced to 4 lbs.
  • the F value was 0.87.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Fats And Perfumes (AREA)

Abstract

L'invention concerne un produit de traitement de trous de forage contenant une phase aqueuse et une phase huileuse non aqueuse, des émulsifiants et éventuellement d'autres additifs comme, par exemple, un agent alourdissant, des additifs de filtrat, des additifs régulateurs de viscosité, des agents mouillants, des sels, biocides, inhibiteurs de corrosion et/ou une réserve alcaline, la phase non aqueuse étant sélectionnée en totalité ou en partie dans le groupe a) des paraffines ayant 5 à 22 atomes de carbone et/ou b) des oléfines internes ayant 12 à 30 atomes de carbone dans la molécule respectivement en mélange avec c) des esters d'acide carboxylique de la formule générale R-C00-R' où R représente un alkyle linéaire ou ramifié, saturé ou non saturé ayant 15 à 25 atomes de carbone et R' représente un alkyle saturé, linéaire ou ramifié ayant 3 à 22 atomes de carbone. L'invention est caractérisée en ce que le quotient de la toxicité d'oléfines internes de la longueur de chaîne C16/C18 (standard IO) et de la toxicité des constituants de la phase non aqueuse qui sont respectivement mesurées selon le test de toxicité des sédiments 96-heures/10 jours statique Leptocheirus plumulosus aigu (selon ASTM E 1367 - 92 & EPA/60018-94/025, section 11), est inférieur à 1.
PCT/EP2003/009981 2002-09-18 2003-09-09 Produit de traitement de trous de forage contenant une phase huileuse a faible toxicite Ceased WO2004029175A1 (fr)

Priority Applications (8)

Application Number Priority Date Filing Date Title
US10/527,212 US7666820B2 (en) 2002-09-18 2003-09-09 Borehole treatment agent containing low-toxic oil phase
MXPA05002670A MXPA05002670A (es) 2002-09-18 2003-09-09 Agente de tratamiento de pozo de sondeo que contiene fase oleosa toxica baja.
EP03769267A EP1546282B1 (fr) 2002-09-18 2003-09-09 Produit de traitement de trous de forage contenant une phase huileuse a faible toxicite
DE50304776T DE50304776D1 (de) 2002-09-18 2003-09-09 Bohrlochbehandlungsmittel mit niedrig-toxischer ölphase
CA002499667A CA2499667A1 (fr) 2002-09-18 2003-09-09 Produit de traitement de trous de forage contenant une phase huileuse a faible toxicite
BRPI0314586-7A BR0314586B1 (pt) 2002-09-18 2003-09-09 Composições de tratamento para furos de sondagem com fase de óleo de baixa toxicidade
AU2003277848A AU2003277848B2 (en) 2002-09-18 2003-09-09 Borehole treatment agent containing low toxic oil phase
NO20051862A NO339445B1 (no) 2002-09-18 2005-04-15 Borehullbehandlingsmidler med en oljefase med lav toksisitet samt anvendelse derav

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10243312A DE10243312A1 (de) 2002-09-18 2002-09-18 Bohrlochbehandlungsmittel mit niedrig-toxischer Ölphase
DE10243312.7 2002-09-18

Publications (1)

Publication Number Publication Date
WO2004029175A1 true WO2004029175A1 (fr) 2004-04-08

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PCT/EP2003/009981 Ceased WO2004029175A1 (fr) 2002-09-18 2003-09-09 Produit de traitement de trous de forage contenant une phase huileuse a faible toxicite

Country Status (10)

Country Link
US (1) US7666820B2 (fr)
EP (1) EP1546282B1 (fr)
AU (1) AU2003277848B2 (fr)
BR (1) BR0314586B1 (fr)
CA (1) CA2499667A1 (fr)
DE (2) DE10243312A1 (fr)
MX (1) MXPA05002670A (fr)
MY (1) MY140131A (fr)
NO (1) NO339445B1 (fr)
WO (1) WO2004029175A1 (fr)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006025521A1 (fr) * 2004-09-03 2006-03-09 Idemitsu Kosan Co., Ltd. Composition d'oléfine interne et huile de base comprenant la composition pour forage pétrolier
WO2007068404A1 (fr) * 2005-12-17 2007-06-21 Cognis Oleochemicals Gmbh Acides ethercarboxyliques en tant qu’additifs pour l’amelioration du pouvoir lubrifiant de solutions de curage a base d’eau
EP1862523A1 (fr) * 2006-06-01 2007-12-05 Cognis Oleochemicals GmbH Fluide de forage à bas toxicité
EP1914288A1 (fr) * 2006-10-20 2008-04-23 Cognis Oleochemicals GmbH Propylalkyl esters utilisés pour la phase oléagineuse des fluids de traitement des puits
EP2053111A1 (fr) * 2007-10-24 2009-04-29 Cognis Oleochemicals GmbH Composition de forage, son processus de préparation, et ses applications
US7718580B2 (en) 2004-09-03 2010-05-18 Idemitsu Kosan Co., Ltd. Internal-olefin composition and base oil comprising the composition for oil drilling
US7807766B2 (en) 2005-09-21 2010-10-05 Cognis Ip Management Gmbh Polymers for use in cleaning compositions

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003093392A1 (fr) * 2002-04-30 2003-11-13 The Petroleum Oil And Gas Corportion Of South Africa (Pty)Ltd Procede pour reduire la toxicite d'hydrocarbones
DE10334441A1 (de) * 2003-07-29 2005-02-17 Cognis Deutschland Gmbh & Co. Kg Bohrlochbehandlungsmittel, enthaltend Ethercarbonsäuren
DE10349808A1 (de) * 2003-10-24 2005-05-25 Cognis Deutschland Gmbh & Co. Kg Emulgatoren für Bohrspülmittel
DE102004034141A1 (de) * 2004-07-15 2006-02-09 Cognis Ip Management Gmbh Verwendung von Lithiumsalzen von Fettalkoholsulfaten zum Reinigen von Bohrlöchern, Bohrgeräten oder Bohrklein
US20080261836A1 (en) * 2007-04-20 2008-10-23 Filler Paul A Compositions for use in well servicing fluids
EP2036963A1 (fr) * 2007-09-14 2009-03-18 Cognis Oleochemicals GmbH Lubrifiants pour fluides de forage
EP2036964A1 (fr) * 2007-09-14 2009-03-18 Cognis Oleochemicals GmbH Epaissisant pour fluides de forage à base d'huile
EP2036962A1 (fr) * 2007-09-14 2009-03-18 Cognis Oleochemicals GmbH Additifs pour fluides de forage à base d'eau
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DE50304776D1 (de) 2006-10-05
NO20051862L (no) 2005-06-14
EP1546282A1 (fr) 2005-06-29
US20070142234A1 (en) 2007-06-21
MY140131A (en) 2009-11-30
DE10243312A1 (de) 2004-04-01
US7666820B2 (en) 2010-02-23
CA2499667A1 (fr) 2004-04-08
MXPA05002670A (es) 2005-05-05
AU2003277848A1 (en) 2004-04-19
NO339445B1 (no) 2016-12-12
AU2003277848B2 (en) 2008-01-10
EP1546282B1 (fr) 2006-08-23
BR0314586B1 (pt) 2014-06-10
BR0314586A (pt) 2005-08-09

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